Do CSF total tau, phosphorylated tau, and β-amyloid 42 help to predict progression of mild cognitive impairment to Alzheimer's disease?: A systematic review and meta-analysis of the literature

被引:108
|
作者
Diniz, Breno S. O. [1 ]
Pinto, Jony A., Jr. [2 ,3 ]
Forlenza, Orestes Vicente [1 ]
机构
[1] Univ Sao Paulo, Neurosci Lab, Fac Med, Dept & Inst Psychiat,LIM 27, BR-05403010 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, CEAPESQ, Inst Psychiat, BR-05403010 Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Inst Math & Stat, BR-05403010 Sao Paulo, SP, Brazil
来源
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY | 2008年 / 9卷 / 03期
关键词
mild cognitive impairment; Alzheimer's disease; CSF biomarkers; beta-amyloid(42); tau;
D O I
10.1080/15622970701535502
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The search for biomarkers as a diagnostic aid to the identification of patients in pre-dementia stages is a fast growing research area. In view of the low specificity attained with the clinically based diagnostic criteria, including those for mild cognitive impairment (MCI), biomarker information will add precision to the incipient dementia diagnostic work-up, particularly Alzheimer's disease (AD). We present a systematic review of the literature and meta-analysis of the most relevant publications about the role of CSF biomarkers in the identification of patients with probable Alzheimer's disease at pre-dementia stages. A total of 16 studies were included in the systematic review, five of which were suitable for meta-analysis. We compared the standard mean differences (SMD) of beta-amyloid 42 (A beta 42), total tau (T-tau) and phosphorylated tau (P-tau) for 130, 169 and 123 patients with MCI who converted to AD (MCI-AD) and 142, 157 and 130 controls, respectively. We conclude that when a clinical diagnosis of MCI is made at baseline assessment, low CSF levels of A beta 42 (SMD: -1.57, CI95% [-2.30 to -0.84], P<0.001), along with high T-tau (SMD: 1.52, CI95% [1.25 to 1.79], P0.001), and high P-tau (SMD: 1.75, CI95% [0.99 to 2.51], P<0.001), help to predict the conversion to Alzheimer's disease as compared to controls subjects.
引用
收藏
页码:172 / 182
页数:11
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